ICD-9 Diagnosis Code 757.39

Skin anomaly NEC

Diagnosis Code 757.39

ICD-9: 757.39
Short Description: Skin anomaly NEC
Long Description: Other specified anomalies of skin
This is the 2014 version of the ICD-9-CM diagnosis code 757.39

Code Classification
  • Congenital anomalies (740–759)
    • Congenital anomalies (740-759)
      • 757 Congenital anomalies of the integument

Information for Medical Professionals

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The ICD-10 and ICD-9 GEMs are used to facilitate linking between the diagnosis codes in ICD-9-CM and the new ICD-10-CM code set. The GEMs are the raw material from which providers, health information vendors and payers can derive specific applied mappings to meet their needs.

  • Acquired perforating pseudoxanthoma elasticum
  • Acquired pseudoxanthoma elasticum
  • Acral Darier's disease
  • Acroerythrokeratoderma
  • Acrokeratosis paraneoplastica of Bazex
  • Acrokeratosis verruciformis of Darier disease
  • Acrokeratosis verruciformis of Hopf
  • Acromegaloid phenotype with cutis verticis gyrata and corneal leukoma
  • Adult junctional epidermolysis bullosa
  • Aplasia cutis congenita
  • Aplasia cutis congenita due to teratogenic drug
  • Aplasia cutis congenita due to underlying malformation
  • Aplasia cutis congenita following intra-uterine infection
  • Aplasia cutis congenita in association with epidermolysis bullosa
  • Aplasia cutis congenita secondary to malformation syndrome
  • Aplasia cutis in Chromosome 4 short-arm deletion syndrome
  • Aplasia cutis in Johanson-Blizzard syndrome
  • Aplasia cutis in Trisomy 13 syndrome
  • Aplasia of skin
  • Arteriovenous malformation of skin
  • Autosomal dominant epidermolysis bullosa simplex
  • Autosomal dominant mutilating keratoderma
  • Autosomal dominant pseudoxanthoma elasticum
  • Autosomal recessive pseudoxanthoma elasticum
  • Bloom syndrome
  • Brugsch's syndrome
  • Bullous eruption of hand
  • Cicatricial junctional epidermolysis bullosa
  • Circumscribed palmoplantar keratoderma
  • Congenital absence of skin on scalp
  • Congenital absence of skin on scalp with epidermal nevi
  • Congenital accessory skin tag
  • Congenital junctional epidermolysis bullosa
  • Congenital junctional epidermolysis bullosa-pyloric atresia syndrome
  • Congenital keratoderma
  • Congenital palmoplantar and perioral keratoderma of Olmsted
  • Congenital scar
  • Conjunctivitis associated with epidermolysis bullosa
  • Cutaneous lesion resulting from spinal dysraphism
  • Cutis verticis gyrata
  • Cutis verticis gyrata with acromegaloid phenotype
  • Deoxyribonucleic acid instability syndrome
  • Diffuse palmoplantar keratoderma of Thost-Unna
  • Disorder of apocrine secretion
  • Dominant dystrophic epidermolysis bullosa
  • Dominant dystrophic epidermolysis bullosa with absence of skin
  • Dominant dystrophic epidermolysis bullosa, albopapular type
  • Dominant epidermolysis bullosa simplex, Weber-Cockayne type
  • Drug-induced epidermolysis bullosa acquisita
  • Drug-induced pseudoxanthoma elasticum
  • Dyskeratosis congenita
  • Dystrophic epidermolysis bullosa
  • Dystrophic epidermolysis bullosa inverse type
  • Emotional sweating affecting palms and soles
  • Epidermolysis bullosa
  • Epidermolysis bullosa acquisita, Brunsting-Perry type
  • Epidermolysis bullosa acquisita, bullous pemphigoid-like
  • Epidermolysis bullosa acquisita, cicatricial pemphigoid-like
  • Epidermolysis bullosa acquisita, classical acral type
  • Epidermolysis bullosa acquisita, oral mucosal involvement
  • Epidermolysis bullosa pruriginosa
  • Epidermolysis bullosa simplex
  • Epidermolysis bullosa simplex of the hands AND/OR feet
  • Epidermolysis bullosa simplex with hypodontia
  • Epidermolysis bullosa simplex with mottled pigmentation
  • Epidermolysis bullosa simplex with neuromuscular disease
  • Epidermolysis bullosa simplex, Ogna type
  • Epidermolysis simplex superficialis
  • Epidermolytic palmoplantar keratoderma of Vorner
  • Erythrokeratoderma
  • Erythrokeratoderma progressiva of Gottron
  • Familial dyskeratotic comedones
  • Flexural Darier's disease
  • Focal dermal hypoplasia
  • Generalized dystrophic epidermolysis bullosa
  • Generalized epidermolysis bullosa simplex
  • Generalized junctional epidermolysis bullosa
  • Generalized recessive dystrophic epidermolysis bullosa mitis
  • Generalized recessive non-mutilating dystrophic epidermolysis bullosa
  • Giant porokeratosis
  • Goltz syndrome
  • Gronblad-Strandberg syndrome
  • Hereditary acantholytic dermatosis
  • Hereditary benign acanthosis nigricans with insulin resistance
  • Hereditary diffuse palmoplantar keratoderma
  • Hereditary erythrokeratolysis
  • Hereditary follicular keratoses
  • Hereditary palmoplantar keratoderma
  • Hypertrophic Darier's disease
  • Hypotrichosis with keratosis pilaris and lentiginosis
  • Hystrix ichthyosis with deafness
  • Ichthyosis hystrix
  • Ichthyosis hystrix gravior of Rheydt
  • Ichthyosis hystrix of Curth-Macklin
  • Inherited disorder of keratinization
  • Inherited epidermolysis bullosa
  • Inherited pseudoxanthoma elasticum
  • Inverse junctional epidermolysis bullosa
  • Junctional epidermolysis bullosa
  • Junctional epidermolysis bullosa gravis of Herlitz
  • Junctional epidermolysis bullosa mitis
  • Juvenile elastoma
  • Keratoderma areata
  • Keratoderma due to Dowling-Meara type epidermolysis bullosa simplex
  • Keratoderma plantare sulcata
  • Keratoderma with deafness
  • Keratoderma with mental retardation and spastic paraplegia
  • Keratoderma with pachyonychia congenita
  • Keratoderma with scleroatrophy of the extremities
  • Keratolysis exfoliativa
  • Keratosis follicularis
  • Keratosis pilaris atrophicans
  • Keratosis pilaris decalvans
  • Keratosis pilaris with ichthyosis and deafness
  • Keratosis rubra pilaris
  • Lethal autosomal recessive epidermolysis bullosa simplex
  • Lichen spinulosus
  • Linear porokeratosis
  • Linear/nevoid/zosteriform Darier's disease
  • Livedo telangiectatica
  • Localized dystrophic epidermolysis bullosa
  • Localized junctional epidermolysis bullosa
  • Localized recessive dystrophic epidermolysis bullosa
  • Lymphedematous keratoderma
  • Maleformatio ectodermalis generalisata of Bafverstedt
  • Mutilating keratoderma
  • Nail dystrophy due to Darier's disease
  • Nevus lipomatosus cutaneous superficialis
  • Pachydermoperiostosis - familial
  • Palmar pitting due to Darier's disease
  • Palmoplantar keratoderma transgrediens
  • Palmoplantar keratoderma with leukoplakia
  • Papuloverrucous palmoplantar keratoderma of Jakac-Wolf
  • Porcupine man
  • Porokeratosis
  • Porokeratosis of Mantoux
  • Porokeratosis of Mibelli
  • Porokeratosis of Mibelli, linear unilateral type
  • Porokeratosis of Mibelli, plaque type
  • Porokeratosis of Mibelli, superficial disseminated type
  • Pretibial epidermolysis bullosa
  • Progressive junctional epidermolysis bullosa
  • Progressive palmoplantar keratoderma of Greither
  • Progressive recessive dystrophic epidermolysis bullosa
  • Pseudoxanthoma elasticum
  • Recessive dystrophic epidermolysis bullosa
  • Relapsing linear acantholytic dermatosis
  • Severe achondrolasia with developmental delay and acanthosis nigricans
  • Symmetrical keratoderma
  • Xeroderma in genetic syndrome

Index of Diseases and Injuries
References found for the code 757.39 in the Index of Diseases and Injuries:

Information for Patients

Skin Conditions

Also called: Cutaneous disorders, Dermatologic disorders

Your skin is your body's largest organ. It covers and protects your body. Your skin

  • Holds body fluids in, preventing dehydration
  • Keeps harmful microbes out, preventing infections
  • Helps you feel things like heat, cold, and pain
  • Keeps your body temperature even
  • Makes vitamin D when the sun shines on it

Anything that irritates, clogs, or inflames your skin can cause symptoms such as redness, swelling, burning, and itching. Allergies, irritants, your genetic makeup, and certain diseases and immune system problems can cause rashes, hives, and other skin conditions. Many skin problems, such as acne, also affect your appearance.

NIH: National Institute of Arthritis and Musculoskeletal and Skin Diseases

  • Acrodermatitis
  • Cradle cap
  • Cryotherapy
  • Cutaneous skin tags
  • Dry skin
  • Dry skin -- self-care
  • Epidermolysis bullosa
  • Erythema multiforme
  • Erythema nodosum
  • Erythema toxicum
  • Granuloma annulare
  • Henoch-Schonlein purpura
  • Ichthyosis vulgaris
  • Intertrigo
  • Ischemic ulcers -- self-care
  • Keratosis pilaris
  • Lichen planus
  • Lichen simplex chronicus
  • Milia
  • Perioral dermatitis
  • Pityriasis rosea
  • Pityriasis rubra pilaris
  • Pyogenic granuloma
  • Sebaceous cyst
  • Seborrheic dermatitis
  • Seborrheic keratosis
  • Skin and hair changes during pregnancy
  • Skin flaps and grafts -- self-care
  • Skin graft
  • Skin lesion biopsy
  • Skin self-exam
  • Stasis dermatitis and ulcers
  • Striae
  • Vesicles
  • Xanthoma
  • Xeroderma pigmentosa

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